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Search Results for " m 9 "

Targets

68

Compounds

6

Natural Products

9

Recombinant Proteins

Cat No. Product Name Synonyms Targets
TP2419 V-9-M Cholecystokinin nonapeptide V 9 M,Prepro CCK Fragment V-9-M,Val-pro-val-glu-ala-val-asp-pro-met,Cholecystokinin Precursor (24-32),V9M,V-9-M Beta Amyloid
V-9-M Cholecystokinin nonapeptide (Prepro CCK Fragment V-9-M) is a precursor compound of cholecystokinin (CCK). Cholecystokinin (CCK) is a brain-intestinal peptide that stimulates gallbladder contraction and pancreatic e...
TP2075L Bombinakinin M acetate Bombinakinin M acetate(509151-65-9 free base) Bradykinin Receptor
Bombinakinin M acetate is a potent bradykinin receptor agonist with high selectivity for mammalian arterial smooth muscle bradykinin receptors and is approximately 50 times more potent than bradykinin.
T18226 M-PEG9-CH2COOH Others , PROTAC Linker
m-PEG9-CH2COOH is a PEG-based PROTAC linker. m-PEG9-CH2COOH can be used in the synthesis of PROTACs.
T18223 M-PEG9-acid Others
m-PEG9-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system withi...
T18224 M-PEG9-Boc Others
m-PEG9-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within...
T18227 M-PEG9-Hydrazide Others
m-PEG9-Hydrazide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system ...
T15940 M-PEG9-Amine Others
m-PEG9-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
T18225 M-PEG9-C4-SH Others
m-PEG9-C4-SH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system with...
T38647 M-PEG9-Br m-PEG9-Br
m-PEG9-Br is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within ...
T38758 M-PEG9-azide m-PEG9-azide
m-PEG9-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system with...
T15941 M-PEG9-phosphonic acid Others
m-PEG9-phosphonic acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome s...
T18229 M-PEG9-SH Others , PROTAC Linker
m-PEG9-SH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within ...
T15932 M-PEG9-NHS ester m-PEG8-CH2CH2-NHS ester Others
m-PEG8-CH2CH2-NHS ester is a PEG--based PROTAC linker can be used in the synthesis of PROTACs.
T18228 M-PEG9-phosphonic acid ethyl ester Others
m-PEG9-phosphonic acid ethyl ester, a PEG-based PROTAC linker, facilitates the synthesis of PROTACs[1].
T18439 N-(m-PEG9)-N'-(propargyl-PEG8)-Cy5 Others
N-(m-PEG9)-N'-(propargyl-PEG8)-Cy5 is a polyethylene glycol (PEG)-based PROTAC linker, specifically designed to aid in the synthesis of PROTACs[1].
T18438 N-(m-PEG9)-N'-(PEG5-acid)-Cy5 Others
N-(m-PEG9)-N'-(PEG5-acid)-Cy5 is a PEG-based PROTAC linker employed for the synthesis of PROTACs[1].
T65860 (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(m-tolyl)propanoic acid
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(m-tolyl)propanoic acid is a useful organic compound for research related to life sciences. The catalog number is T65860 and the CAS number is 211637-74-0.
T8756 KRAS inhibitor-9 DUN09716 Apoptosis , Ras
KRAS inhibitor-9 (DUN09716) is a potent KRAS inhibitor with Kd of 92 μM that blocks the formation of GTP-KRAS and downstream activation of KRAS. KRAS inhibitor-9 causes G2/M cell cycle arrest and induces apoptosis. KRAS ...
T16750 Rigosertib ON-01910 Apoptosis , FLT , PLK , PI3K , Bcr-Abl , CDK , PDGFR , Src
Rigosertib (ON-01910) is a selective and non-ATP-competitive inhibitor of PLK1 (IC50: 9 nM). Rigosertib is a multi-kinase inhibitor and a selective anti-cancer agent, which induces apoptosis by inhibition of the PI3 kina...
T28449 Pradefovir ICN-2001-3,MB-6866,ICN-20013,MB-06866,Remofovir HBV
Pradefovir (Remofovir) is a reverse transcriptase inhibitor potentially for treatment of chronic HBV infection. Pradefovir is also a liver-targeted prodrug of adefovir. After metabolic activation, Pradefovir was converte...
T5818 Rigosertib sodium Rigosertib,Estybon,ON-01910 Apoptosis , PLK , PI3K
Rigosertib sodium (ON-01910), a non-ATP-competitive inhibitor of PLK1(IC50=9 nM), exhibits 30-fold higher specificity activity over Plk2 and no effect on Plk3.
T62567 CDK2-IN-9
CDK2-IN-9 is a potent inhibitor of CDK2 (IC50: 0.63 μM) with anti-proliferative effects. CDK2-IN-9 is capable of blocking the cell cycle in S and G2/M phases and inducing apoptosis. CDK2-IN-9 has potential for melanoma r...
T61935 B-Raf IN 9
B-Raf IN 9 (compound 8b) is an effective B-Raf inhibitor (IC50=24.79 nM). B-Raf IN 9 blocks cell cycle at G2/M phase and induces apoptosis. B-Raf IN 9 showed potent anti-tumor activity on human prostate cancer PC-3 cells...
T62217 Tubulin polymerization-IN-9
Tubulin polymerization-IN-9 is a potent inhibitor of tubulin (IC50: 1.82 μM). Tubulin polymerization-IN-9 arrests the cell cycle of K562 cells in G2/M phase and induces apoptosis and mitochondrial depolarization. Tubulin...
TP1350 H-Val-Pro-Pro-OH TFA (58872-39-2 free base) H-Val-Pro-Pro-OH TFA
H-Val-Pro-Pro-OH(TFA), a proline peptide derivative from milk, is an ACE inhibitor with IC50 of 9 M.
T74621 STING agonist-9
STING Agonist-9 (Compound 45) is a powerful stimulator of the STING pathway, demonstrating potent activity with an EC50 of 1.2 nM against human STING (h-STING) and 32.82 μM against mouse STING (m-STING). It exhibits anti...
T63304 Topoisomerase II inhibitor 9
Topoisomerase II inhibitor 9 is a Topo II inhibitor (IC50: 0.97 μM) and DNA embedding agent (IC50: 43.51 μM) that blocks the Hep G-2 cell cycle in the G2/M phase and induces apoptosis.
T61779 STAT3-IN-9
STAT3-IN-9, a potent inhibitor of STAT3 activation at Tyr705, exhibits no impact on the phosphorylation of STAT1 at Tyr 701. Additionally, this compound efficiently induces apoptosis and cell cycle arrest specifically at...
TP1054 PACAP (1-38), human, ovine, rat TFA Pituitary Adenylate Cyclase Activating Polypeptide 38 (TFA)
PACAP (1-38), a novel neuropeptide isolated from the bovine hypothalamus is more active than vasoactive intestinal peptide (VIP) in stimulating adenylate cyclase (EC50=7 nM). PACAP 1-38 (10-9 M) increased substance P (SP...
T70527 DAT-230
DAT-230 is a promising microtubule inhibitor that has great potential for the treatment of fibrosarcoma in vitro and in vivo. DAT-230 exhibited potent anti-proliferative activity against various cancer cells. DAT-230 -tr...
T28092 MPT0B206
MPT0B206 is a novel tubulin polymerization inhibitor. MPT0B206 induced G2/M cell cycle arrest and the appearance of the mitotic marker MPM-2 in K562 and K562R cells, which is associated with the upregulation of cyclin B1...
T76041 GIP (1-30) amide,human acetate
GIP (1-30) amide, human acetate is a fragment of glucose-dependent insulinotropic polypeptide (GIP), an incretin hormone that plays a crucial role in stimulating insulin secretion and mitigating postprandial glycemic exc...
T37713 Funalenone
Funalenone is a phenalenone originally isolated from A. niger. It inhibits HIV-1 integrase (IC50 = 10 μM) and HIV-1 replication in human peripheral blood cells transformed by murine leukemia virus (HPB-M(a); IC50 = 1.7 μ...
T61673 Anticancer agent 56
Anticancer agent 56 (compound 4d) is a powerful anti-cancer compound with favorable drug-like properties. It shows significant anticancer activity against multiple cancer cell lines, with an IC50 value of less than 3 μM....
TP1662 Galanin Receptor Ligand M35
The chimeric peptide M35 [galanin (1-13)-bradykinin(2-9) amide] is a high-affinity galanin receptor ligand acting as a galanin receptor antagonist in the rat spinal cord, rat hippocampus and isolated mouse pancreatic isl...
T35998 3,5-Dihydroxybenzaldehyde
3,5-Dihydroxybenzaldehyde is a building block.1,2It has been used in the synthesis of 2,4-dimethylbenzoylhydrazones with antileishmanial and antioxidant activities. 1.Taha, M., Baharudin, M.S., Ismail, N.H., et al.Synthe...
T71217 MPT0B214
MPT0B214 is a novel and potent microtubule inhibitor with potential anticancer activity. MPT0B214 inhibited tubulin polymerization through strongly binding to the tubulin's colchicine-binding site and had cytotoxic activ...
T36844 Inostamycin A
Inostamycin A is a bacterial metabolite that has been found inStreptomycesand has anticancer activity.1It is an inhibitor of CDP-diacylglycerol:inositol 3-phosphatidyltransferase (IC50= 0.02 μg/ml in A431 cell membranes)...
T35423 7-oxo Staurosporine
7-oxo Staurosporine is an antibiotic originally isolated from S. platensis with diverse biological activites. It inhibits PKC, PKA, phosphorylase kinase, EGFR, and c-Src in vitro (IC50s = 9, 26, 5, 200, and 800 nM, respe...
T37002 7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate (ammonium salt)
7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate (SBD-F) is a thiol-reactive fluorogenic probe.1It has been used to quantify the levels of homocysteine, cysteine, and cysteamine in human plasma.2SBD-F displays excitation/emissi...
T37692 Piericidin B
Piericidin B is a bacterial metabolite that has been found inS. mobaraensisand has insecticidal and antimicrobial activities.1,2,3It inhibits NADH oxidase activity in isolated bovine heart mitochondria and inhibits respi...
T37674 Aspyrone
Aspyrone is a polyketide fungal metabolite that has been found inAspergillusand has diverse biological activities.1,2It is active against a panel of 13 fungi when used at a concentration of 20 μg/ml and a panel of 21 bac...
T37062 L-Leucine-7-amido-4-methylcoumarin hydrochloride
L-Leu-AMC is a fluorogenic substrate for leucine aminopeptidase.1Upon enzymatic cleavage by leucine aminopeptidase, AMC is released and its fluorescence can be used to quantify leucine aminopeptidase activity. AMC displa...
T35504 (±)10-HDHA
(±)10-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro.[1][2] It is also produced from incubations of DHA in rat liver, brain, and intestinal microsomes.[3][4][5] (±)10-HDHA is a potential marker of...
T35975 6,9-Dichloro-1,2,3,4-tetrahydroacridine
6,9-Dichloro-1,2,3,4-tetrahydroacridine is a synthetic intermediate in the synthesis of tacrine-based acetylcholinesterase (AChE) inhibitors.1It is also an intermediate in the synthesis of multifunctional tacrine hybrids...
T35680 2-(1-(Thiophen-2-yl)ethylidene)hydrazinecarbothioamide
2-(1-(Thiophen-2-yl)ethylidene)hydrazinecarbothioamide is an antimicrobial agent.1It is active against the Gram-negative bacteriaE. coli,P. aeruginosa, andS. marcescens(MICs = 64, 100, and 70 μg/ml, respectively), the Gr...
T36174 Methyl 3,4-Dihydroxyphenylacetate
Methyl 3,4-dihydroxyphenylacetate is a polyphenol that has been found inI. aquifoliumseeds and has antioxidant and antiviral activities.1,2It scavenges 2,2-diphenyl-1-picrylhydrazyl radicals in a cell-free assay (IC50= 0...
T36053 D-Lysine lactam
D-Lysine lactam is a chiral building block.1,2It has been used in the synthesis of a chiral antibiotic synthetic intermediate, as well as in the stereoselective synthesis of neurokinin (NK) receptor antagonists. 1.Kumar,...
T37721 Dihydronovobiocin
Dihydronovobiocin is a coumarin antibiotic and derivative of novobiocin .1It is active against the bacteriaS. aureus,S. haemolyticus,D. pneumoniae,S. typhosa,K. pneumoniae, andP. multocida(MICs = 0.6, 2, 0.6, 10, 10, and...
T35762 MC1742
MC1742 is an inhibitor of class I histone deacetylases (HDACs; IC50s = 0.1, 0.11, 0.02, and 0.61 μM for HDAC1, -2, -3, and -8, respectively) and class IIb HDACs (IC50s = 7 and 40 nM for HDAC6 and HDAC10, respectively).1 ...

Compounds

V-9-M Cholecystokinin nonapeptide
TP2419
Synonym: V 9 M,Prepro CCK Fragment V-9-M,Val-pro-val-glu-ala-val-asp-pro-met,Cholecystokinin Precursor (24-32),V9M,V-9-M
Target: Beta Amyloid
Bombinakinin M acetate
TP2075L
Synonym: Bombinakinin M acetate(509151-65-9 free base)
Target: Bradykinin Receptor
m-PEG9-CH2COOH
T18226
Synonym:
Target: Others, PROTAC Linker
m-PEG9-acid
T18223
Synonym:
Target: Others
m-PEG9-Boc
T18224
Synonym:
Target: Others
m-PEG9-Hydrazide
T18227
Synonym:
Target: Others
m-PEG9-Amine
T15940
Synonym:
Target: Others
m-PEG9-C4-SH
T18225
Synonym:
Target: Others
m-PEG9-Br
T38647
Synonym: m-PEG9-Br
Target:
m-PEG9-azide
T38758
Synonym: m-PEG9-azide
Target:
m-PEG9-phosphonic acid
T15941
Synonym:
Target: Others
m-PEG9-SH
T18229
Synonym:
Target: Others, PROTAC Linker
m-PEG9-NHS ester
T15932
Synonym: m-PEG8-CH2CH2-NHS ester
Target: Others
m-PEG9-phosphonic acid ethyl ester
T18228
Synonym:
Target: Others
N-(m-PEG9)-N'-(propargyl-PEG8)-Cy5
T18439
Synonym:
Target: Others
N-(m-PEG9)-N'-(PEG5-acid)-Cy5
T18438
Synonym:
Target: Others
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(m-tolyl)propanoic acid
T65860
Synonym:
Target:
KRAS inhibitor-9
T8756
Synonym: DUN09716
Target: Apoptosis, Ras
Rigosertib
T16750
Synonym: ON-01910
Target: Apoptosis, FLT, PLK, PI3K, Bcr-Abl, CDK, PDGFR, Src
Pradefovir
T28449
Synonym: ICN-2001-3,MB-6866,ICN-20013,MB-06866,Remofovir
Target: HBV
Rigosertib sodium
T5818
Synonym: Rigosertib,Estybon,ON-01910
Target: Apoptosis, PLK, PI3K
CDK2-IN-9
T62567
Synonym:
Target:
B-Raf IN 9
T61935
Synonym:
Target:
Tubulin polymerization-IN-9
T62217
Synonym:
Target:
H-Val-Pro-Pro-OH TFA (58872-39-2 free base)
TP1350
Synonym: H-Val-Pro-Pro-OH TFA
Target:
STING agonist-9
T74621
Synonym:
Target:
Topoisomerase II inhibitor 9
T63304
Synonym:
Target:
STAT3-IN-9
T61779
Synonym:
Target:
PACAP (1-38), human, ovine, rat TFA
TP1054
Synonym: Pituitary Adenylate Cyclase Activating Polypeptide 38 (TFA)
Target:
DAT-230
T70527
Synonym:
Target:
MPT0B206
T28092
Synonym:
Target:
GIP (1-30) amide,human acetate
T76041
Synonym:
Target:
Funalenone
T37713
Synonym:
Target:
Anticancer agent 56
T61673
Synonym:
Target:
Galanin Receptor Ligand M35
TP1662
Synonym:
Target:
3,5-Dihydroxybenzaldehyde
T35998
Synonym:
Target:
MPT0B214
T71217
Synonym:
Target:
Inostamycin A
T36844
Synonym:
Target:
7-oxo Staurosporine
T35423
Synonym:
Target:
7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate (ammonium salt)
T37002
Synonym:
Target:
Piericidin B
T37692
Synonym:
Target:
Aspyrone
T37674
Synonym:
Target:
L-Leucine-7-amido-4-methylcoumarin hydrochloride
T37062
Synonym:
Target:
(±)10-HDHA
T35504
Synonym:
Target:
6,9-Dichloro-1,2,3,4-tetrahydroacridine
T35975
Synonym:
Target:
2-(1-(Thiophen-2-yl)ethylidene)hydrazinecarbothioamide
T35680
Synonym:
Target:
Methyl 3,4-Dihydroxyphenylacetate
T36174
Synonym:
Target:
D-Lysine lactam
T36053
Synonym:
Target:
Dihydronovobiocin
T37721
Synonym:
Target:
MC1742
T35762
Synonym:
Target:
1 2
Cat No. Product Name Synonyms Targets
T0062 Folic acid Folate,Vitamin B9,Pteroylglutamic acid,Vitamin M,Folacin DNA/RNA Synthesis , Endogenous Metabolite
Folic acid (Vitamin B9)(Vitamin M; Vitamin B9) is indispensable for the production and maintenance of new cells, for DNA/RNA synthesis.
T5S1952 9-Methoxycamptothecin Apoptosis , Topoisomerase
9-Methoxycamptothecin (MCPT) has antitumour activities through topoisomerase inhibition.
TN5336 9-Oxo-10,11-dehydroageraphorone 4,7(11)-Cadinadiene-3,8-dione,DTD,7,11-Dehydro-8-oxoageraphorone
9-Oxo-10,11-dehydroageraphorone has acaricidal activity. It induces hepatotoxicity and cholestasis in rats. 9-Oxo-10,11-dehydroageraphorone also effectively inhibits the proliferation of HeLa cells by arresting the cell ...
T14121 Actinonin (-)-Actinonin Aminopeptidase
Actinonin ((-)-Actinonin) is a naturally occurring antibacterial agent produced by Actinomyces and a potent reversible peptide deformylase (PDF) inhibitor with a Ki of 0.28 nM, it also is an apoptosis inducer. Actinonin ...
T37272 9(S),12(S),13(S)-TriHOME
9(S),12(S),13(S)-TriHOME is a linoleic acid-derived oxylipin that has diverse biological activities.1,2,3,4It has been found in various plants and is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble ...
T36348 Cerebroside C
Cerebroside C is a fungal metabolite and glycosphingolipid that has been found in the rice pathogenic fungusM. grisea.1It induces production of the phytoalexin momilactone A when applied to wounded rice leaves, indicatin...

Recombinant Proteins

Cat No. Product Name Species Expression System
TMPY-03343 EIF3K Protein, Human, Recombinant (His & GST) Human Baculovirus Insect Cells
EIF3K is a member of the eIF3 subunit K family. It is a component of the eukaryotic translation initiation factor 3 (eIF-3) complex, which is required for several steps in the initiation of protein synthesis. The eIF-...
TMPJ-00865 VEGF121 Protein, Human, Recombinant (His) Human HEK293 Cells
Human VEGF121, also known as Vascular endothelial growth factor A, VEGFA, Vascular permeability factor, VPF and VEGF, is a homodimeric, heparin-binding glycoprotein which belongs to the platelet-derived growth factor (PD...
TMPY-03698 VEGF121b Protein, Human, Recombinant Human HEK293 Cells
VEGF121b Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 34.10 kDa and the accession number is P15692-9.
TMPH-00005 YAP1 Protein, Human, Recombinant (Isoform 9, His) Human P. pastoris (Yeast)
YAP1 Protein, Human, Recombinant (Isoform 9, His) is expressed in yeast with C-6xHis tag. The predicted molecular weight is 56.4 kDa; 80 kDa, reducing conditions and the accession number is P46937-9.
TMPY-00818 Granzyme H/GZMH Protein, Human, Recombinant (His) Human HEK293 Cells
Granzymes are key components of the immune response that play important roles in eliminating host cells infected by intracellular pathogens. Several granzymes are potent inducers of cell death. A total of eight granzymes...
TMPH-02613 ATF-5 Protein, Mouse, Recombinant (His & Myc) Mouse E. coli
Transcription factor that either stimulates or represses gene transcription through binding of different DNA regulatory elements such as cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3'), ATF5-specific respo...
TMPK-00825 VEGF121 Protein, Human, Recombinant (His & Avi) Human HEK293 Cells
Vascular endothelial growth factor (VEGF or VEGF-A), also known as vascular permeability factor (VPF), is a potent mediator of both angiogenesis and vasculogenesis in the fetus and adult. VEGF165 appears to be the most a...
TMPK-00826 VEGF121 Protein, Human, Recombinant (His & Avi), Biotinylated Human HEK293 Cells
Vascular endothelial growth factor (VEGF or VEGF-A), also known as vascular permeability factor (VPF), is a potent mediator of both angiogenesis and vasculogenesis in the fetus and adult. VEGF165 appears to be the most a...
TMPY-05268 Neurofascin Protein, Human, Recombinant (hFc), Biotinylated Human HEK293 Cells
Neurofascin Protein, Human, Recombinant (hFc), Biotinylated is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 130 kDa and the accession number is O94856-9.
TargetMol